gudid
Primary ID: 802 012
N/A (UDI 802 012)
Manufactured by inomed Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 802 012
Device Regulatory Overview
The N/A (Model/Catalog Number: 802 012) is a medical device manufactured by inomed Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 802 012
- Product Code / EMDN
- DZP
- Device Name
- ZD probe holder with micrometer advancefor instruments up to 3mm
- Database Sync Date
- 2026-08-09 09:07:45
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of N/A?
The registered manufacturer of record for N/A is inomed Medizintechnik GmbH.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 802 012.
What classification code is assigned to this device?
This device is registered under product classification code DZP.
Similar Classification Devices (DZP)
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